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IL110278A0 - Enzymatic processes for the resolution of enantiomeric mixtures - Google Patents

Enzymatic processes for the resolution of enantiomeric mixtures

Info

Publication number
IL110278A0
IL110278A0 IL11027894A IL11027894A IL110278A0 IL 110278 A0 IL110278 A0 IL 110278A0 IL 11027894 A IL11027894 A IL 11027894A IL 11027894 A IL11027894 A IL 11027894A IL 110278 A0 IL110278 A0 IL 110278A0
Authority
IL
Israel
Prior art keywords
resolution
enzymatic processes
enantiomeric mixtures
enantiomeric
mixtures
Prior art date
Application number
IL11027894A
Other versions
IL110278A (en
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of IL110278A0 publication Critical patent/IL110278A0/en
Publication of IL110278A publication Critical patent/IL110278A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02—Oxygen as only ring hetero atoms
    • C12P17/04—Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/16—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing two or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/004—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of alcohol- or thiol groups in the enantiomers or the inverse reaction
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/005—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/822—Microorganisms using bacteria or actinomycetales
    • Y10S435/874—Pseudomonas
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/921—Candida
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/939—Rhizopus

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
IL110278A 1993-07-14 1994-07-11 Enzymatic processes for the resolution of enantiomeric mixtures of azetidinone derivatives IL110278A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US9217093A 1993-07-14 1993-07-14

Publications (2)

Publication Number Publication Date
IL110278A0 true IL110278A0 (en) 1994-10-21
IL110278A IL110278A (en) 1998-06-15

Family

ID=22231980

Family Applications (1)

Application Number Title Priority Date Filing Date
IL110278A IL110278A (en) 1993-07-14 1994-07-11 Enzymatic processes for the resolution of enantiomeric mixtures of azetidinone derivatives

Country Status (12)

Country Link
US (2) US5879929A (en)
EP (1) EP0634492A1 (en)
JP (1) JPH0775595A (en)
KR (1) KR960014352A (en)
CN (1) CN1100144A (en)
AU (1) AU688766B2 (en)
CA (1) CA2127972A1 (en)
FI (1) FI943326A7 (en)
HU (1) HU217790B (en)
IL (1) IL110278A (en)
SG (1) SG54231A1 (en)
TW (1) TW397866B (en)

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JPS60501995A (en) * 1983-08-11 1985-11-21 キヤロル，ノエル Liquid separation method and device
US5602272A (en) * 1994-06-21 1997-02-11 Bristol-Myers Squibb Company Reduction and resolution methods for the preparation of compounds useful as intemediates for preparing taxanes
US5635531A (en) * 1996-07-08 1997-06-03 Bristol-Myers Squibb Company 3'-aminocarbonyloxy paclitaxels
EP1308519B1 (en) * 1997-01-24 2006-04-19 Sumitomo Chemical Company, Limited Process for improving optical purity of azetidine-2-carboxylic acid
GB9714877D0 (en) * 1997-07-15 1997-09-17 Chiroscience Ltd Microorganism and its use
EP1054996B1 (en) 1998-02-17 2004-01-28 G.D. SEARLE & CO. Process for the enzymatic resolution of lactams
JP3757629B2 (en) * 1998-07-17 2006-03-22 住友化学株式会社 Process for producing optically active N-substituted azetidine-2-carboxylic acid compound
AU6049000A (en) * 1999-07-23 2001-02-13 Eli Lilly And Company Enantioselective acylation of cis racemic azetidinones
HK1049787B (en) 1999-10-01 2014-07-25 Immunogen, Inc. Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents
US6548293B1 (en) * 1999-10-18 2003-04-15 Fsu Research Foundation, Inc. Enzymatic process for the resolution of enantiomeric mixtures of β-lactams
KR20010112393A (en) 2000-02-02 2001-12-20 플로리다 스테이트 유니버시티 리서치 파운데이션, 인크 C7 Heterosubstituted Acetate Taxanes as Antitumor Agents
CZ20013405A3 (en) 2000-02-02 2002-03-13 Florida State University Research Foundation, Inc. C10 carbonate substituted taxanes functioning as antitumor agents
BR0104350A (en) 2000-02-02 2002-01-02 Univ Florida State Res Found Heterosubstituted c10 acetate taxanes as antitumor agents
AR030188A1 (en) * 2000-02-02 2003-08-13 Univ Florida State Res Found TAXANO COMPOUNDS REPLACED WITH ESTERS IN C7; PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND PROCESS TO TREAT A MAMMER SUBJECT THAT SUFFERS FROM A CONDITION THAT RESPONDS TO TAXANS
CZ20013521A3 (en) 2000-02-02 2002-03-13 Florida State University Research Foundation, Inc. C7 carbamoyloxy substituted taxanes functioning as antitumor substances
HK1047936A1 (en) * 2000-02-02 2003-03-14 佛罗里达州立大学研究基金有限公司 C10 carbamoyloxy substituted taxanes as antitumor agents
PL350315A1 (en) 2000-02-02 2002-12-02 Univ Florida State Res Found C7 carbonate substituted taxanes as antitumor agents
US6649632B2 (en) 2000-02-02 2003-11-18 Fsu Research Foundation, Inc. C10 ester substituted taxanes
JP2004512838A (en) * 2000-11-02 2004-04-30 シーエスアイアール Process for producing (-)-menthol and its analogous compounds
EP1375495B1 (en) * 2001-03-07 2008-09-03 Daiichi Sankyo Company, Limited Method for producing a 2-azetidinone derivative
US7064980B2 (en) * 2003-09-17 2006-06-20 Sandisk Corporation Non-volatile memory and method with bit line coupled compensation
PE20050693A1 (en) * 2004-02-13 2005-09-27 Univ Florida State Res Found TAXANS REPLACED WITH CYCLOPENTIL ESTERS IN C10
CN1960721A (en) 2004-03-05 2007-05-09 佛罗里达州立大学研究基金有限公司 C7 lactyloxy-substituted taxanes
WO2006088767A2 (en) * 2005-02-14 2006-08-24 Florida State University Research Foundation, Inc. C10 cyclopropyl ester substituted taxane compositions
JP2011517455A (en) * 2008-03-31 2011-06-09 フロリダ・ステイト・ユニバーシティ・リサーチ・ファウンデイション・インコーポレイテッド C (10) ethyl ester and C (10) cyclopropyl ester substituted taxanes

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US4492757A (en) * 1981-12-28 1985-01-08 Denki Kagaku Kogyo Kabushiki Kaisha Process for preparing L-threonine
JPS60248192A (en) * 1984-05-23 1985-12-07 Sumitomo Chem Co Ltd Preparation of optically active threo-3-phenylserine derivative
FR2629819B1 (en) * 1988-04-06 1990-11-16 Rhone Poulenc Sante PROCESS FOR THE PREPARATION OF BACCATIN III AND DESACETYL-10 BACCATIN III DERIVATIVES
US4943528A (en) * 1988-11-22 1990-07-24 Nitto Chemical Industry Co., Ltd. Process for the production of optically active (R)-(-)-3-halo-1,2-propanediol
JPH02190195A (en) 1989-01-19 1990-07-26 Rikagaku Kenkyusho Method for producing optically active propionic acid ester compounds
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EP0582469A2 (en) * 1992-08-06 1994-02-09 Wisconsin Alumni Research Foundation Process for preparing taxol-type compound from beta-lactam precursors
MX9308012A (en) * 1992-12-24 1994-08-31 Bristol Myers Squibb Co PHOSPHONOOXIMETHYL ETHER OF TAXANE DERIVATIVES, SOLUBLE IN WATER AND PHARMACEUTICAL COMPOSITIONS INCLUDING THEM.

Also Published As

Publication number Publication date
CA2127972A1 (en) 1995-01-15
HU217790B (en) 2000-04-28
EP0634492A1 (en) 1995-01-18
US5879929A (en) 1999-03-09
KR960014352A (en) 1996-05-22
HUT69958A (en) 1995-09-28
TW397866B (en) 2000-07-11
HU9402096D0 (en) 1994-09-28
AU6743394A (en) 1995-01-27
IL110278A (en) 1998-06-15
US6541242B1 (en) 2003-04-01
FI943326A7 (en) 1995-01-15
FI943326A0 (en) 1994-07-12
CN1100144A (en) 1995-03-15
JPH0775595A (en) 1995-03-20
SG54231A1 (en) 1998-11-16
AU688766B2 (en) 1998-03-19

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